Suppr超能文献

[冯雷克林霍增氏神经纤维瘤病与皮肤黑素细胞痣]

[Von Recklinghausen neurofibromatosis and dermal melanocytic nevi].

作者信息

Tanner M, Proksch E, Christophers E

机构信息

Hautklinik, Christian-Albrechts-Universität zu Kiel.

出版信息

Hautarzt. 1995 Apr;46(4):263-7. doi: 10.1007/s001050050252.

Abstract

Neurofibromas, café au lait macules and freckles in the axillary or inguinal regions are common manifestations of von Recklinghausen's neurofibromatosis (NF-1). Less known is the simultaneous appearance of dermal melanocytic naevi. We describe the case of a 21-year-old Vietnamese woman who showed generalized, multiple neurofibromas, a solitary plexiform neurofibroma in the left gluteal region and Lisch nodules. In addition, there were several large grey-blue macules histologically characterized by fusiform pigment-bearing cells in the dermis, which we diagnosed as persistent aberrant mongolian spots. In the right zygomatic region she presented a grey-blue, hair-bearing macule, which we saw as a variant of Ota's naevus. A genetic background for this coincidence of a systemic with a local phakomatosis can be supposed, as both Schwann's cells and melanocytes are derived from the neural crest. Such pathologic rearrangement in the embryogenesis of the cellular elements could be important for the pathogenesis of NF-1 and dermal melanocytic nevi.

摘要

神经纤维瘤、咖啡斑以及腋窝或腹股沟区域的雀斑是冯·雷克林豪森神经纤维瘤病(NF-1)的常见表现。皮肤黑素细胞痣同时出现则较为少见。我们报道了一例21岁越南女性病例,该患者有全身多发性神经纤维瘤、左侧臀区一个孤立的丛状神经纤维瘤以及Lisch结节。此外,还有几个大的灰蓝色斑,组织学特征为真皮内梭形含色素细胞,我们诊断为持续性异常蒙古斑。在右侧颧部区域,她有一个灰蓝色、有毛发的斑,我们认为这是太田痣的一种变异型。鉴于施万细胞和黑素细胞均起源于神经嵴,因此可以推测这种系统性与局部错构瘤病的巧合存在遗传背景。细胞成分胚胎发育中的这种病理重排可能对NF-1和皮肤黑素细胞痣的发病机制具有重要意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验